Canonical Allele Identifier: CA2680562358

Gene: CITED2

Linked Data

• gnomAD v4: 6-139372876-A-AAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372879_139372882dup , CM000668.2:g.139372879_139372882dup	GRCh38
NC_000006.11:g.139694016_139694019dup , CM000668.1:g.139694016_139694019dup	GRCh37
NC_000006.10:g.139735709_139735712dup	NCBI36
NG_016169.1:g.6769_6772dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*252_*255dup MANE Select	ENSP00000356623.2:n.*252_*255dup
ENST00000367651.3:c.*252_*255dup	ENSP00000356623.2:n.*252_*255dup
ENST00000536159.2:c.*252_*255dup	ENSP00000442831.1:n.*252_*255dup
ENST00000537332.2:c.*252_*255dup	ENSP00000444198.2:n.*252_*255dup
NM_001168388.2:c.*252_*255dup	NP_001161860.1:n.*252_*255dup
NM_001168389.2:c.*252_*255dup	NP_001161861.2:n.*252_*255dup
NM_006079.4:c.*252_*255dup	NP_006070.2:n.*252_*255dup
NM_006079.5:c.*252_*255dup MANE Select	NP_006070.2:n.*252_*255dup
NM_001168388.3:c.*252_*255dup	NP_001161860.1:n.*252_*255dup
NM_001168389.3:c.*252_*255dup	NP_001161861.2:n.*252_*255dup